Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.
Summary Literature (1)
DOID:0050453 - lissencephaly


Disease Ontology Definition:A congenital nervous system abnormality characterized by the absence of folds in the cerebral cortex and caused_by defective neuronal migration during the 12th to 24th weeks of gestation.

Synonyms:

Xenbase Genes : arx, reln, dcx, pafah1b1, nde1, lamb1, tuba1cl.3, tuba1a

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0018838 - lissencephaly spectrum disorders

OMIM:
OMIM:300067 - LISSENCEPHALY, X-LINKED, 1; LISX1
OMIM:300215 - LISSENCEPHALY, X-LINKED, 2; LISX2
OMIM:607432 - LISSENCEPHALY 1; LIS1
OMIM:611603 - LISSENCEPHALY 3; LIS3
OMIM:614019 - LISSENCEPHALY 4; LIS4
OMIM:615191 - LISSENCEPHALY 5; LIS5

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): congenital nervous system abnormality (is_a)